Sunitinib Sandoz sunitinib 12.5 mg capsule blister Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sunitinib sandoz sunitinib 12.5 mg capsule blister

sandoz pty ltd - sunitinib, quantity: 12.5 mg - capsule - excipient ingredients: titanium dioxide; povidone; microcrystalline cellulose; iron oxide red; gelatin; mannitol; magnesium stearate; croscarmellose sodium; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; shellac; strong ammonia solution; sulfuric acid - ? treatment of advanced renal cell carcinoma (rcc),? treatment of gastrointestinal stromal tumour (gist) after failure of imatinib mesilate treatment due to resistance or intolerance,? treatment of unresectable, well-differentiated pancreatic neuroendocrine tumours (pancreatic net).

Sunitinib Sandoz sunitinib 25 mg capsule bottle Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sunitinib sandoz sunitinib 25 mg capsule bottle

sandoz pty ltd - sunitinib, quantity: 25 mg - capsule - excipient ingredients: magnesium stearate; gelatin; croscarmellose sodium; mannitol; povidone; microcrystalline cellulose; iron oxide red; titanium dioxide; iron oxide yellow; iron oxide black; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; shellac; strong ammonia solution; sulfuric acid - ? treatment of advanced renal cell carcinoma (rcc),? treatment of gastrointestinal stromal tumour (gist) after failure of imatinib mesilate treatment due to resistance or intolerance,? treatment of unresectable, well-differentiated pancreatic neuroendocrine tumours (pancreatic net).

Sunitinib Sandoz sunitinib 25 mg capsule blister Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sunitinib sandoz sunitinib 25 mg capsule blister

sandoz pty ltd - sunitinib, quantity: 25 mg - capsule - excipient ingredients: gelatin; croscarmellose sodium; magnesium stearate; microcrystalline cellulose; povidone; mannitol; titanium dioxide; iron oxide red; iron oxide yellow; iron oxide black; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; shellac; strong ammonia solution; sulfuric acid - ? treatment of advanced renal cell carcinoma (rcc),? treatment of gastrointestinal stromal tumour (gist) after failure of imatinib mesilate treatment due to resistance or intolerance,? treatment of unresectable, well-differentiated pancreatic neuroendocrine tumours (pancreatic net).

Sunitinib Sandoz sunitinib 37.5 mg capsule blister Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sunitinib sandoz sunitinib 37.5 mg capsule blister

sandoz pty ltd - sunitinib, quantity: 37.5 mg - capsule - excipient ingredients: povidone; gelatin; microcrystalline cellulose; magnesium stearate; mannitol; titanium dioxide; croscarmellose sodium; iron oxide yellow; propylene glycol; butan-1-ol; isopropyl alcohol; purified water; strong ammonia solution; ethanol absolute; iron oxide black; ethanol; shellac; sulfuric acid - ? treatment of advanced renal cell carcinoma (rcc),? treatment of gastrointestinal stromal tumour (gist) after failure of imatinib mesilate treatment due to resistance or intolerance,? treatment of unresectable, well-differentiated pancreatic neuroendocrine tumours (pancreatic net).

Sunitinib Sandoz sunitinib 50 mg capsule blister Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sunitinib sandoz sunitinib 50 mg capsule blister

sandoz pty ltd - sunitinib, quantity: 50 mg - capsule - excipient ingredients: gelatin; titanium dioxide; croscarmellose sodium; magnesium stearate; microcrystalline cellulose; iron oxide red; povidone; mannitol; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; shellac; strong ammonia solution; sulfuric acid - ? treatment of advanced renal cell carcinoma (rcc),? treatment of gastrointestinal stromal tumour (gist) after failure of imatinib mesilate treatment due to resistance or intolerance,? treatment of unresectable, well-differentiated pancreatic neuroendocrine tumours (pancreatic net).

Sunitinib Sandoz sunitinib 12.5 mg capsule bottle Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sunitinib sandoz sunitinib 12.5 mg capsule bottle

sandoz pty ltd - sunitinib, quantity: 12.5 mg - capsule - excipient ingredients: magnesium stearate; mannitol; gelatin; iron oxide red; microcrystalline cellulose; povidone; croscarmellose sodium; titanium dioxide; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; shellac; strong ammonia solution; sulfuric acid - ? treatment of advanced renal cell carcinoma (rcc),? treatment of gastrointestinal stromal tumour (gist) after failure of imatinib mesilate treatment due to resistance or intolerance,? treatment of unresectable, well-differentiated pancreatic neuroendocrine tumours (pancreatic net).

SANDOZ VENLAFAXINE XR venlafaxine (as hydrochloride) 150 mg modified release capsule blister pack Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sandoz venlafaxine xr venlafaxine (as hydrochloride) 150 mg modified release capsule blister pack

alembic pharmaceuticals australia pty ltd - venlafaxine hydrochloride, quantity: 169.8 mg (equivalent: venlafaxine, qty 150 mg) - capsule, modified release - excipient ingredients: gelatin; ethylcellulose; sunset yellow fcf; povidone; magnesium stearate; microcrystalline cellulose; brilliant blue fcf; copovidone; allura red ac; purified talc; colloidal anhydrous silica; titanium dioxide; propylene glycol; ethanol; isopropyl alcohol; shellac; tert-butyl alcohol; sodium hydroxide - sandoz venlafaxine xr is indicated for the treatment of: - major depression, including prevention of relapse and recurrence where appropriate; - generalised anxiety disorder; - social anxiety disorder; panic disorder, including prevention of relapse.

SANDOZ VENLAFAXINE  XR venlafaxine (as hydrochloride) 75 mg modified release capsule blister pack Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sandoz venlafaxine xr venlafaxine (as hydrochloride) 75 mg modified release capsule blister pack

alembic pharmaceuticals australia pty ltd - venlafaxine hydrochloride, quantity: 84.9 mg (equivalent: venlafaxine, qty 75 mg) - capsule, modified release - excipient ingredients: iron oxide black; colloidal anhydrous silica; ethylcellulose; iron oxide red; magnesium stearate; microcrystalline cellulose; povidone; purified talc; titanium dioxide; gelatin; copovidone; propylene glycol; butan-1-ol; isopropyl alcohol; purified water; shellac; ethanol absolute; ammonia - sandoz venlafaxine xr is indicated for the treatment of: - major depression, including prevention of relapse and recurrence where appropriate; - generalised anxiety disorder; - social anxiety disorder; panic disorder, including prevention of relapse.